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The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as
The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as
The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma
The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma
We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s
We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s
The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i
The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i
Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under
Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under
Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD
Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD
Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under
Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under
Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa
Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir
Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder
Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder
The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates sta
The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates sta
IQVIA is expanding its team and is seeking a Retail & Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated
IQVIA is expanding its team and is seeking a Retail & Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated
Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. Th
Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. Th
